ENST00000706989.1:c.2152A>C
|
ENSP00000516702.1:p.Asn718His
|
|
ENST00000359125.7:c.2098A>C
MANE Select
|
ENSP00000352035.2:p.Asn700His
|
|
ENST00000637193.1:c.1495A>C
|
ENSP00000490734.1:p.Asn499His
|
|
ENST00000344462.8:c.2005A>C
|
ENSP00000339611.4:p.Asn669His
|
|
ENST00000357249.6:c.1666A>C
|
ENSP00000349789.3:p.Asn556His
|
|
ENST00000359125.6:c.2098A>C
|
ENSP00000352035.2:p.Asn700His
|
|
ENST00000360480.7:c.2014A>C
|
ENSP00000353668.3:p.Asn672His
|
|
ENST00000370224.5:c.2122A>C
|
ENSP00000359244.2:p.Asn708His
|
|
ENST00000625514.2:c.2086A>C
|
ENSP00000486040.1:p.Asn696His
|
|
ENST00000626839.2:c.2044A>C
|
ENSP00000486706.1:p.Asn682His
|
|
ENST00000629241.2:c.2014A>C
|
ENSP00000487142.1:p.Asn672His
|
|
ENST00000629676.2:c.1679+6285A>C
|
ENSP00000486194.1:n.1679+6285A>C
|
|
NM_004518.4:c.2014A>C
|
NP_004509.2:p.Asn672His
|
|
NM_172106.1:c.2044A>C
|
NP_742104.1:p.Asn682His
|
|
NM_172107.2:c.2098A>C
|
NP_742105.1:p.Asn700His
|
|
NM_172108.3:c.2005A>C
|
NP_742106.1:p.Asn669His
|
|
XM_006723787.1:c.2140A>C
|
XP_006723850.1:p.Asn714His
|
|
XM_011528807.1:c.2206A>C
|
XP_011527109.1:p.Asn736His
|
|
XM_011528808.1:c.2203A>C
|
XP_011527110.1:p.Asn735His
|
|
XM_011528809.1:c.2176A>C
|
XP_011527111.1:p.Asn726His
|
|
XM_011528810.1:c.2152A>C
|
XP_011527112.1:p.Asn718His
|
|
XM_011528811.1:c.2122A>C
|
XP_011527113.1:p.Asn708His
|
|
XM_011528812.1:c.2095A>C
|
XP_011527114.1:p.Asn699His
|
|
XM_011528813.1:c.2080A>C
|
XP_011527115.1:p.Asn694His
|
|
XM_011528814.1:c.1687A>C
|
XP_011527116.1:p.Asn563His
|
|
NM_004518.5:c.2014A>C
|
NP_004509.2:p.Asn672His
|
|
NM_172106.2:c.2044A>C
|
NP_742104.1:p.Asn682His
|
|
NM_172107.3:c.2098A>C
|
NP_742105.1:p.Asn700His
|
|
NM_172108.4:c.2005A>C
|
NP_742106.1:p.Asn669His
|
|
XM_011528810.2:c.2152A>C
|
XP_011527112.1:p.Asn718His
|
|
XM_011528811.2:c.2122A>C
|
XP_011527113.1:p.Asn708His
|
|
XM_017027841.2:c.2149A>C
|
XP_016883330.1:p.Asn717His
|
|
XM_017027842.2:c.2086A>C
|
XP_016883331.1:p.Asn696His
|
|
XM_017027843.1:c.2083A>C
|
XP_016883332.1:p.Asn695His
|
|
XM_017027844.2:c.2041A>C
|
XP_016883333.1:p.Asn681His
|
|
XM_017027845.1:c.1114A>C
|
XP_016883334.1:p.Asn372His
|
|
NM_004518.6:c.2014A>C
|
NP_004509.2:p.Asn672His
|
|
NM_172106.3:c.2044A>C
|
NP_742104.1:p.Asn682His
|
|
NM_172107.4:c.2098A>C
MANE Select
|
NP_742105.1:p.Asn700His
|
|
NM_172108.5:c.2005A>C
|
NP_742106.1:p.Asn669His
|
|
NM_001382235.1:c.2152A>C
|
NP_001369164.1:p.Asn718His
|
|